Transferrin-Conjugated Liposome/IL-12 pDNA Complexes for Cancer Gene Therapy in Mice

  • Joo, Soo-Yeon (College of Pharmacy, Sookmyung Women's University) ;
  • Kim, Jin-Seok (College of Pharmacy, Sookmyung Women's University) ;
  • Park, Heon-Joo (Department of Microbiology, College of Medicine, Inha University) ;
  • Choi, Eun-Kyung (Department of Radiation Oncology, University of Ulsan)
  • Published : 2005.08.31

Abstract

Transferrin ($T_{f}$) has been used as a targeting ligand for delivering liposome/interleukin-12 (IL-12) pDNA complexes to cancer cells mostly due to the greater number of transferrin receptors ($T_{f}R$) found on tumor cells than on normal cells. $T_{f}$ was conjugated to liposomes via the reaction of MPB-PE with thiol groups of $T_{f}$ introduced by a heterobifunctional cross-linking agent, N-succinimidyl-3-(2-pyridyldithio)propionate (SPDP). Four days after C26 inoculation when the tumor volume reached ${\sim}100mm^{3}$, tumor-bearing Balb/c mice were injected intravenously with $T_{f}-liposome/IL-12 pDNA$complexes twice a week for 3 weeks. Significant suppression of tumor growth was achieved in the group treated with the $T_{f}-liposome/IL-12 pDNA$ complexes, with a dose of $10{\mu}g$ of IL-12 pDNA showing the highest suppression effect among the tested doses. Similar results were obtained when the therapy was initiated one day after tumor inoculation, although in this case $30{\mu}g$ IL-12 pDNA/$T_{f}-liposome$ complexes showed a significant suppression of tumor growth between 19 and 23 days after tumor inoculation. This result indicates that the transferrin receptor-targeted liposomal system is an efficient delivery agent of therapeutic genes, such as IL-12, in mice and that its potential clinical use warrants further research investigation.

Keywords

References

  1. M. S. Wadhwa, D. L. Knoell, A. P. Young, and K. G. Rice, Bioconjug. Chem., 6, 283 (1995) https://doi.org/10.1021/bc00033a008
  2. T. Friedmann, Science, 244, 1275 (1989) https://doi.org/10.1126/science.2660259
  3. R. C. Mulligan, Science, 260, 926 (1993) https://doi.org/10.1126/science.8493530
  4. J. Han, S. K. Kim, T. S. Cho, and H. S. Joung, Macromol. Res., 12, 501 (2004) https://doi.org/10.1007/BF03218434
  5. X. Gao and L. Huang, Gene Ther., 2, 710 (1995)
  6. R. I. Mahato, A. Rolland, and E. Tomlinson, Pharm. Res., 14, 853 (1997) https://doi.org/10.1023/A:1012187414126
  7. P. Cheng, Hum. Gene Ther., 7, 275 (1996) https://doi.org/10.1089/hum.1996.7.3-275
  8. T. Miyamoto, N. Tanaka, Y. Eishi, and T. Amagasa, Int. J. Oral Maxillofac. Sug. (Denmark), 23, 430 (1994) https://doi.org/10.1016/S0901-5027(05)80039-6
  9. R. I. Elliot, M. C. Elliot, F. Wang, and J. F. Head, Ann. NY Acad. Sci., 698, 159 (1993) https://doi.org/10.1111/j.1749-6632.1993.tb17204.x
  10. K. Thorstensen and I. Romslo, Scand. J. Clin. Lab. Invest. Suppl. (Norway), 215, 113 (1993)
  11. A. Sartori, X. MA, G. Gri, L. Showe, D. Benjamin, and G. Trinchieri, Methods, 11, 116 (1997) https://doi.org/10.1006/meth.1996.0395
  12. G. Trinchieri, Blood, 84, 4008 (1994)
  13. H. Tahara and M.T. Lotze, Gene Ther., 2, 96 (1995)
  14. F. Cavallo, P. Signorelli, M. Giovarelli, P. Musiani, A. Modesti, and G. Forni, J. Natl. Cancer Inst., 89, 1049 (1997)
  15. M. J. Brunda, J. Exp. Med., 178, 1223 (1993) https://doi.org/10.1084/jem.178.4.1223
  16. J. Tan, C. A. Newton, J. Y. Djeu, D. E. Gutsh, A. E. Chang, N. S. Yang, T. W. Klein, and H. Yu, Cancer Res., 56, 3399 (1996)
  17. Y. Iwanuma, F. A. Chen, N. K. Egilmez, H. Takita, and R. B. Bankert, Cancer Res., 57, 2937 (1997)
  18. S. Majewski, M. Marzak, A. Szmurlo, S. Jablonska, and W. Bollag, J. Invest. Dermatol., 106, 1114 (1996) https://doi.org/10.1111/1523-1747.ep12340161
  19. Y. Yoshida, K. Takasi, M. Kimurai, K. Takenega, and H. Yamamoto, Anticancer Res., 18, 333 (1998)
  20. M. J. Brunda, J. Leukocyte Biol., 55, 280 (1994) https://doi.org/10.1002/jlb.55.2.280
  21. M. J. Brunda, L. Luistro, P. R. Warrier, R. B. Wright, B. R. Hubbard, M. Murphy, and S. F. Wolf, J. Exp. Med., 178, 1223 (1993) https://doi.org/10.1084/jem.178.4.1223
  22. Y. Noguchi, E. C. Richards, Y. T. Chen, and L. J. Old, Proc. Natl. Acad. Sci., USA, 92, 2219 (1995)
  23. T. Tada, S. Ohzeki, K. Utsumi, H. Takiuchi, M. Muramatsu, X. F. Li, J. Shimizu, H. Fujiwara, and T. Hamaoka, J. Immunol., 146, 1077 (1991)
  24. D. J. Verbik, W. W. Stinson, M. J. Brunda, A. Kessinger, and S. S. Joshi, Clin. Exp. Metastasis, 14, 219 (1996)
  25. S. Y. Joo and J. S. Kim, Drug Dev. Ind. Pharm., 28, 1023 (2002) https://doi.org/10.1081/DDC-120006433
  26. F. J. Martin and D. Papahadjopoulos, J. Biol. Chem., 257, 286 (1982)
  27. F. Szoka and D. Papadjopoulos, Proc. Natl. Acad. Sci., USA, 75, 4194 (1978)
  28. J. Carlsson, H. Drevin, and R. Axen, Biochem. J., 173, 723 (1978) https://doi.org/10.1042/bj1730723
  29. F. J. Martin, T. D. Heath, and R. R. C. New, Liposomes: A Practical Approach, R.R.C. New, Ed., IRL Press, Oxford, 1990, p. 163
  30. T. H. Corbett and D. P. Griswold, Cancer Chemother. Rep., 5, 169 (1975)